PRRT2
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 16[11]
- Cytogenetic location
- 16p11.2[15]
- Expressed in
- right hemisphere of cerebellum, cerebellar vermis, right frontal lobe, Brodmann area 9, primary visual cortex, middle temporal gyrus, prefrontal cortex, superior frontal gyrus, nucleus accumbens, cingulate gyrus[16][17][18][19][20][21][22][23][24][25]
- Found in taxon
- Homo sapiens[10]
- Genetic association
- benign familial infantile epilepsy, Infantile convulsions and choreoathetosis[12][13]
- HomoloGene ID
- 114328[3]
- Strand orientation
- forward strand[14]
🏷️ Also known as
en PRRT2
en BFIC2
en BFIS2
en DSPB3
en DYT10
en EKD1
en FICCA
en ICCA
en IFITMD1
en PKC
en proline rich transmembrane protein 2
ar PRRT٢
🔖 Identifiers · 11
- Ensembl gene ID
- ENSG00000167371
- Ensembl transcript ID
- ENST00000572820, ENST00000300797, ENST00000358758, ENST00000562148, ENST00000567551, ENST00000567659, ENST00000568516, ENST00000636001, ENST00000636019, ENST00000636131, ENST00000636246, ENST00000636619, ENST00000636902, ENST00000637064, ENST00000637290, ENST00000637403, ENST00000637425, ENST00000637542, ENST00000637565, ENST00000637596, ENST00000647876
- Entrez Gene ID
- 112476
- Exact match
- identifiers.org
- Freebase ID
- /m/0hnct93
- HGNC ID
- 30500
- HGNC gene symbol
- PRRT2
- Microsoft Academic ID (discontinued)
- 2781402956
- OMIM ID
- 614386
- RefSeq RNA ID
- NM_001256442, NM_001256443, NM_145239, XM_011545715, XM_017022887, XM_017022888, XM_017022889
- UMLS CUI
- C1826724
🔗 Connections
Expressed in 7
Chromosome 1
Found in taxon 1
Instance of 1
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